D
Dehai Li
Researcher at Chinese Ministry of Education
Publications - 246
Citations - 5155
Dehai Li is an academic researcher from Chinese Ministry of Education. The author has contributed to research in topics: Chemistry & Medicine. The author has an hindex of 36, co-authored 218 publications receiving 3832 citations. Previous affiliations of Dehai Li include Ocean University of China & University of British Columbia.
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New alkaloids and diterpenes from a deep ocean sediment derived fungus Penicillium sp.
TL;DR: In this article, four new alkaloids, including two new meleagrin analogs and two new diketopiperazines, including roquefortines F (5) and G (6), together with six new diterpenes, conidiogenones B-G (7−12), were isolated from a deep ocean sediment derived fungus Penicillium sp.
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Antiviral isoindolone derivatives from an endophytic fungus Emericella sp. associated with Aegiceras corniculatum.
TL;DR: Chemical investigation of the endophytic fungus Emericella sp.
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Antiviral alkaloids produced by the mangrove-derived fungus Cladosporium sp. PJX-41.
TL;DR: Six new indole alkaloids including five new glyantrypine derivatives and a new pyrazinoquinazoline derivative and four known alkaloid derivatives were isolated from the culture of the mangrove-derived fungus Cladosporium sp.
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Phenylspirodrimanes with anti-HIV activity from the sponge-derived fungus stachybotrys chartarum mxh-x73
TL;DR: Seven new phenylspirodrimanes, named stachybotrins D-F, stachybocins E and F, and stachybosides A and B, and four known compounds, were isolated from the sponge-derived fungus Stachybotrys chartarum MXH-X73, and compound 1 showed an inhibitory effect on HIV-1 replication by targeting reverse transcriptase.
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Aspulvinones from a mangrove rhizosphere soil-derived fungus Aspergillus terreus Gwq-48 with anti-influenza A viral (H1N1) activity
Huquan Gao,Wenqiang Guo,Qiang Wang,Lianqing Zhang,Meilin Zhu,Tianjiao Zhu,Qianqun Gu,Wei Wang,Dehai Li +8 more
TL;DR: Only compound 1 exhibited effective inhibitory activity against H1N1 viral neuraminidase (NA), and docking of two isomers into the active sites of NA showed that the E double bond Δ(5(10)) was essential to achieve activity.